51 to 75 of 94 Permanent GMP Jobs in the UK excluding London

company dedicated to improving health and wellness through cutting-edge products. Committed to excellence, they operate to the highest standards of Good Manufacturing Practices (GMP). Key Responsibilities: Oversee and maintain the Quality Management System (QMS) to ensure compliance with GMP standards. Conduct thorough internal audits and participate in external … reviews to identify areas for improvement and ensure continuous quality enhancement. Collaborate with cross-functional teams to implement quality processes and provide training on GMP compliance. Develop and update quality policies, procedures, and documentation to align with industry best practices. Requirements: Bachelor's degree in a relevant field (e.g., Life … Sciences, Pharmacy, Quality Management). Proven experience in quality systems management within the Medical Nutrition or Pharmaceutical industries. In-depth knowledge of GMP standards and regulatory requirements. Strong analytical skills with a keen eye for detail. Excellent communication and interpersonal abilities to work effectively with various teams. Experience in leading more »

QA role in Pharma R&D, Infrastructure and Validation team, you will perform the quality assurance activities and quality oversight of the Validation and GMP facilities management activities performed within Pharma R&D across the UK sites. In this role you will be key in the following areas… • Providing review more »

profile and past history: 1. Relevant degree in a chemistry related discipline. 2. Proven industry experience in development activities for drug development in a GMP environment. 3. A working knowledge and practical experience with management of an analytical chemistry function/facility in the pharmaceutical industry. Hyper Recruitment Solutions Ltd more »

safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift ... more »

p As a leader within the Manufacturing, Science & Tech (MS&T) organisation with accountability to ensure the Seed Manufacturing department maintains the highest GMP standards. You will develop and maintain a healthy and high performing team, which executes the strategic plan to consistently deliver high quality products in a compliant … our Liverpool site./p p b Responsibilities/b/p ul li Ensure the consistent attainment of company standards in relation to GMP - right first-time execution, accurate data, timely close out of Deviation Reporting (DR’s), Corrective and Preventative actions (CAPA), Change Control, aseptic practices and housekeeping more »

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

Undertake other duties in relation to the position as the Company requires, including working additional hours as requested by the Systems Delivery Manager Ensure GMP is adhered to in all areas of work. Understand Company’s Health & Safety Policy and follow all company HSE procedures.Report all accidents or any unsafe more »

URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR. Execution and approval of the corresponding protocols to release the required equipment for GMP production Weekly Validation Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects more »

part of the process. Engage regularly with multi disciplined teams/training and mentoring. Worked within an Automotive/Pharmaceutical/Medical device/GMP environment. Bachelors degree or equivalent in Engineering. DMAIC (desirable). Lean/Six Sigma qualifications. Travel requirements; Travel between local manufacturing sites is required – no more »

Facilitate flow of information with Quality and Finance departments. Supporting the Supply Chain and Operations to enable that all assets, processes and procedures meet GMP/GDP requirements. Maintain a complete understanding of the flow to ensure an efficient process. Be able to translate forecasts into production schedules, batch allocations more »

fixed weekly rotation. Responsibilities: Perform routine quality control examinations. Conduct routine analysis of raw materials and products using various techniques. Ensure all work is GMP compliant. Use a variety of instrumental and wet chemistry techniques to ensure analysis is accurate. Ensure consistent production of high-quality self-care products. Key more »

interpretation, knowledge, and experience for project direction and delivery. Support process scale-up and material supply delivery in labs and pilot plant areas, including GMP clinical trial material production as per business needs. Responsible for ensuring and driving compliance in all safety and quality aspects of process development activities. If more »

on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »

and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare professionals, community pharmacies, patients, and wholesalers. Ensuring the completion of checks for new products; having the appropriate more »

a capable and robust/stable process. Adhere to Quality Management System (QMS) requirements in line with Corin’s ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820. Support brainstorming and problem-solving as required activities for inspection processes and assist in resolving engineering/manufacturing problems, as well more »

development. Work with the project and business development managers from receipt of RFPS to develop firm proposals and subsequent project delivery. Ensure current Good Manufacturing Practice (cGMP) compliance. Maintain a safe working environment compliant with all relevant Environment, Health and Safety (EHS) requirements. Maintain and expand the cGMP QC services … and product specifications, Certificates of testing, Stability Study Protocols, Method Qualification Protocols and Reports. Manage the ongoing environmental monitoring and water testing of the GMP facility and operation. Manage the investigation of out-of-trend (OOT), out-of-specification (OOS) and any deviation events. Ensure that all regulatory expectations are … met regarding any GMP QC samples or data collected, manipulated, reported, stored or archived. Provide timely and accurate testing updates for materials, samples, products and stability studies to internal parties and external clients. Has budgetary responsibility for the QC department including management of spend and equipment capital expenditure ensuring development more »

co-ordinate the day to day workload, ensuring items are manufactured in a timely manner and colleagues are supported. To follow good manufacturing practice (GMP) at all times. To generate worksheets and labels, ensuring medicines are charged correctly using the pharmacy computer system. To in process check worksheets and labels more »

of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply more »

Job summary The Vaccine Development and Evaluation Centre department, based at UKHSA Porton, is the UK's largest capability for the handling of dangerous human pathogens and animal modelling of infectious diseases. The capability is used to understand pathogenesis and more »

under of 'specials' licence. You will have a key role in ensuring all units with Pharmacy Technical Services are compliant to Good Manufacturing Practice (GMP). About us University Hospitals Bristol and Weston NHS Foundation Trust (UHBW) is one of the largest acute Trusts in the country, bringing together a … responsibilities, please refer to the job description document attached to this vacancy. Person Specification Knowledge and Experience Essential Basic knowledge of Good Manufacturing Practice (GMP) Basic knowledge of Good QC Laboratory Practice (GQCLP) Experience of working in a laboratory undertaking analysis Desirable Experience of aseptic preparation Knowledge of COSHH & health more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and more »

being made correctly Write reports on the analysis carried out for CofAs. Ensure that the testing done is carried out to the required standard (GMP, GLP, MHRA etc). What do you need to be considered? You will need: Degree or equivalent experience in science-based subject, ideally Chemistry. Working … Experience of analysing organic compounds such as fine chemicals, petrochemicals, or APIs. Knowledge of working in a regulated laboratory and standards such as UKAS, GMP, GLP, MHRA, FDA etc. What to do next? Interested? Of course you are, who wouldnt want to work for a great company with a supportive more »

for the benefit of the service. Interview date: 8th July 2024 Main duties of the job To ensure that all current Good Manufacturing Practice (GMP) Quality Assurance activities are effectively managed to meet agreed Trust and Pharmacy Department objectives whilst complying will all relevant national and local legislation, regulations and more »

of Validation Proven leadership skills. Computer literate with the ability to use CRM systems Experience and knowledge of H&S, COSHH, ISO, GLP and GMP A problem solver Due to the nature of the role, you will need excellent colour vision If you believe you meet the above criteria and more »